2,5,7-Trihydroxy-3-(4-methoxyphenyl)-2,3-dihydrochromen-4-one

Details

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Internal ID eab62d42-daf9-4b49-9be4-007f2aadc0b7
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 4-O-methylated isoflavonoids
IUPAC Name 2,5,7-trihydroxy-3-(4-methoxyphenyl)-2,3-dihydrochromen-4-one
SMILES (Canonical) COC1=CC=C(C=C1)C2C(OC3=CC(=CC(=C3C2=O)O)O)O
SMILES (Isomeric) COC1=CC=C(C=C1)C2C(OC3=CC(=CC(=C3C2=O)O)O)O
InChI InChI=1S/C16H14O6/c1-21-10-4-2-8(3-5-10)13-15(19)14-11(18)6-9(17)7-12(14)22-16(13)20/h2-7,13,16-18,20H,1H3
InChI Key IIQJLBKXWGKSKE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H14O6
Molecular Weight 302.28 g/mol
Exact Mass 302.07903816 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 1.78
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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IIQJLBKXWGKSKE-UHFFFAOYSA-N

2D Structure

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2D Structure of 2,5,7-Trihydroxy-3-(4-methoxyphenyl)-2,3-dihydrochromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9522 95.22%
Caco-2 + 0.6669 66.69%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.7645 76.45%
OATP2B1 inhibitior - 0.7225 72.25%
OATP1B1 inhibitior + 0.9218 92.18%
OATP1B3 inhibitior + 0.8662 86.62%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8637 86.37%
P-glycoprotein inhibitior - 0.8611 86.11%
P-glycoprotein substrate - 0.9463 94.63%
CYP3A4 substrate + 0.5525 55.25%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8139 81.39%
CYP3A4 inhibition + 0.5165 51.65%
CYP2C9 inhibition + 0.6650 66.50%
CYP2C19 inhibition + 0.6521 65.21%
CYP2D6 inhibition - 0.8380 83.80%
CYP1A2 inhibition + 0.7188 71.88%
CYP2C8 inhibition - 0.6795 67.95%
CYP inhibitory promiscuity + 0.7329 73.29%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5780 57.80%
Eye corrosion - 0.9808 98.08%
Eye irritation + 0.5862 58.62%
Skin irritation - 0.6220 62.20%
Skin corrosion - 0.9523 95.23%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7366 73.66%
Micronuclear + 0.9300 93.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.9582 95.82%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.6418 64.18%
Acute Oral Toxicity (c) III 0.6358 63.58%
Estrogen receptor binding + 0.6162 61.62%
Androgen receptor binding + 0.7795 77.95%
Thyroid receptor binding + 0.6525 65.25%
Glucocorticoid receptor binding + 0.7199 71.99%
Aromatase binding + 0.6045 60.45%
PPAR gamma + 0.5785 57.85%
Honey bee toxicity - 0.8915 89.15%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9250 92.50%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.82% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.04% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.24% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.01% 96.09%
CHEMBL1929 P47989 Xanthine dehydrogenase 92.86% 96.12%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.36% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.16% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.08% 99.23%
CHEMBL4208 P20618 Proteasome component C5 87.98% 90.00%
CHEMBL1951 P21397 Monoamine oxidase A 87.71% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.90% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.71% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.11% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.18% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 84.07% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.97% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.20% 99.17%
CHEMBL2581 P07339 Cathepsin D 82.99% 98.95%
CHEMBL3194 P02766 Transthyretin 81.86% 90.71%
CHEMBL2535 P11166 Glucose transporter 80.97% 98.75%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.45% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.38% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Trifolium subterraneum

Cross-Links

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PubChem 9904478
LOTUS LTS0261024
wikiData Q105113691